All day Allergy d

Product NDC

0904-5831

11-digit product format

009045831

Labeler code

0904

Product ID

0904-5831_58653567-2d66-4f26-b5c3-54677bfb5cb3

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine HCl, Pseudoephedrine HCl

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Major Pharmaceuticals

Application

ANDA077170

Marketing category

ANDA

Marketing start

2008-05-06

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

Active strength

5 mg/1; mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record